Gómez M C, Pope C E, Dresser B L
Audubon Nature Institute Center for Research of Endangered Species, New Orleans, LA 70131, USA.
Theriogenology. 2006 Jul 1;66(1):72-81. doi: 10.1016/j.theriogenology.2006.03.017. Epub 2006 Apr 18.
Nuclear transfer (NT) technology is typically used for generating identical individuals, but it is also a powerful resource for understanding the cellular and molecular aspects of nuclear reprogramming. Most recently, the procedure has been used in humans for producing patient-specific embryonic stem cells. The successful application of NT in cats was demonstrated by the birth of domestic and non-domestic cloned kittens at a similar level of efficiency to that reported for other mammalian species. In cats, it has been demonstrated that either in vivo or in vitro matured oocytes can be used as donor cytoplasts. The length of in vitro oocyte maturation affects in vitro development of reconstructed embryos, and oocytes matured in vitro for shorter periods of time are the preferred source of donor cytoplasts. For NT, cat somatic cells can be synchronized into the G0/G1 phase of the cell cycle by using different methods of cell synchronization without affecting the frequency of in vitro development of cloned embryos. Also, embryo development to the blastocyst stage in vitro is not influenced by cell type, but the effect of cell type on the percentage of normal offspring produced requires evaluation. Inter-species NT has potential application for preserving endangered felids, as live offspring of male and female African wildcats (AWC, Felis silvestris lybica) have been born and pregnancies have been produced after transferring black-footed cat (Felis nigripes) cloned embryos into domestic cat (Felis silvestris catus) recipients. Also, successful in vitro embryo development to the blastocyst stage has been achieved after inter-generic NT of somatic cells of non-domestic felids into domestic cat oocytes, but no viable progeny have been obtained. Thus, while cat cytoplasm induces early nuclear remodeling of cell nuclei from a different genus, the high incidence of early embryo developmental arrest may be caused by abnormal nuclear reprogramming. Fetal resorption and abortions were frequently observed at various stages of pregnancy after transfer of AWC cloned embryos into domestic cat recipients. Abnormalities, such as abdominal organ exteriorization and respiratory failure and septicemia were the main causes of death in neonatal cloned kittens. Nonetheless, several live domestic and AWC cloned kittens have been born that are seemingly normal and healthy. It is important to continue evaluating these animals throughout their lives and to examine their capability for natural reproduction.
核移植(NT)技术通常用于克隆相同的个体,但它也是了解细胞核重编程细胞和分子层面的有力资源。最近,该技术已在人类中用于生产患者特异性胚胎干细胞。NT技术在猫身上的成功应用体现在家猫和非家猫克隆小猫的诞生,其效率与其他哺乳动物物种报道的水平相近。在猫中,已证明体内或体外成熟的卵母细胞均可用作供体细胞质。体外卵母细胞成熟的时长会影响重构胚胎的体外发育,体外成熟时间较短的卵母细胞是供体细胞质的首选来源。对于NT而言,通过不同的细胞同步方法可使猫体细胞同步进入细胞周期的G0/G1期,且不会影响克隆胚胎的体外发育频率。此外,胚胎体外发育至囊胚阶段不受细胞类型影响,但细胞类型对正常后代产生百分比的影响有待评估。种间核移植在保护濒危猫科动物方面具有潜在应用价值,因为将黑足猫(Felis nigripes)克隆胚胎移植到家猫(Felis silvestris catus)受体后,已诞生雄性和雌性非洲野猫(AWC,Felis silvestris lybica)的活体后代并成功受孕。同样,将非家猫科动物的体细胞与家猫卵母细胞进行属间核移植后,胚胎在体外成功发育至囊胚阶段,但尚未获得存活后代。因此,虽然猫的细胞质可诱导不同属细胞核的早期核重塑,但早期胚胎发育停滞的高发生率可能是由异常的核重编程导致的。将非洲野猫克隆胚胎移植到家猫受体后,在妊娠的各个阶段经常观察到胎儿吸收和流产现象。异常情况,如腹部器官外露、呼吸衰竭和败血症是新生克隆小猫死亡的主要原因。尽管如此,仍有几只看似正常健康的家猫和非洲野猫克隆小猫出生。持续评估这些动物的一生并检查它们的自然繁殖能力很重要。